CLINICAL CASE O THE EFFECTIVE TREATMENT OF RELAPSE OF ANAPLASTIC PLEOMORPHIC XANTHOASTROCYTOMA WITH BRAF V600E MUTATION USING TARGET DRUG VEMURAFENIB


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Abstract

Pleomorphic xanthoastrocytomas are rare glial tumors. They account for less than 1% of the cerebral astrocytomas. Pleomorphic xanthoastrocytomas are low-grade glial tumors, namely, 2nd grade according to WHO classification. In some cases, however, anaplastic pleomorphic xanthoastrocytomas may develop, and they are characterized by a more aggressive course, frequent relapses, like high-grade cerebral gliomas brain (anaplastic astrocytoma or glioblastoma). BRAF V600 mutation in tumor occurs in 30-40% of cases of anaplastic pleomorphic xanthoastrocytoma. Presented clinical case demonstrates the ability to achieve long-term remission using B-raf inhibitor vemurafenib in the treatment of patient with relapses of anaplastic pleomorphic xanthoastrocytoma and with the V600E BRAF mutation in tumor. It is necessary to conduct clinical studies of BRAF inhibitors in patients with anaplastic pleomorphic xanthoastrocytomas with the presence of BRAF V600 mutations in tumor.

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About the authors

D. R Naskhletashvili

Email: nas-david@yandex.ru
PhD, Senior Scientist at the Neurosurgical (Oncological) Department FSBI RORC n.a. N.N. Blokhin of RMH Moscow

References

  1. Lee E.Q., Ruland S., LeBoeuf N.R., et al. Successful Treatment of a Progressive BRAF V600E-Mutated Anaplastic Pleomorphic Xanthoastrocytoma With Vemurafenib Monotherapy. J. Clin. Oncol. 2016;34(10):87.
  2. Fouladi M., Jenkins J., Burger P., Langston J., Merchant T., Heideman R., Thompson S., Sanford A., Kun L. Pleomorphic xanthoastrocytoma: favorable outcome after complete surgical resection. Neurooncol. 2016;3: 184-92.
  3. Giannini C., Scheithauer B.W., Burger P.C., Brat D.J., Wolan R.C., Lach B., O'Neill B.P. Pleomorphic xanthoastrocytoma: what do we really know about it? Cancer. 1999;85: 2033-45.
  4. Kepes J.J., Rubinstein L.G., Eng L.F. Pleomorphic xanthoastrocytoma:adistinctivemeningocerebral glioma of young subjects with relatively favorable prognosis: a study of 12 cases. Cancer. 1979;44: 1839-52.
  5. Kieran M.W. Phase 1 study of dabrafenib in pediatric patients (pts) with relapsed or refractory BRAF V600E high- and low-grade gliomas (HGG, LGG), Langerhans cell histiocytosis (LCH), and other solid tumors (OST). 2015 ASCO Ann. Meeting, abstract 10004.
  6. Kieran M.W., Cohen K.J., Doz F., Dunkel I.J., Hargrave D.R., et al. Complete radiographic responses in pediatric patients with BRAFV600-positive tumors including high-grade gliomas: Preliminary results of an ongoing phase 1/2a safety and pharmacokinetics (PK) study of dabrafenib. J. Clin. Oncol. 2014;32(Suppl; abstr 10056):5.
  7. Munoz E.L., Eberhard D.A., Lopes M.B.S., Schneider B.F., Gonzales F., VandenBerg S.R. Proliferative activity and p53 mutation as prognostic indicators in pleomorphic xanthoasrocytoma. J. Neuropathol. Exp. Neurol. 1996;55:606.
  8. Pahapill P.A., Ramsey D.A., Del Maestro R.F. Pleomorphic xanthoastrocytoma: case report and analysis of the literature concerning the efficacy of resection and the significance of necrosis. Neurosurgery. 199;28:606-9.

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